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Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report
The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation. This disease falls within the scope of a McCune-Albright syndrome in less than 7 % of cases. The authors reported the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569405/ https://www.ncbi.nlm.nih.gov/pubmed/33102631 http://dx.doi.org/10.1016/j.ejro.2019.12.002 |
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author | Bile-Gui, Lynda N. Ahoury, Judicael Kabas, Raïssa M. |
author_facet | Bile-Gui, Lynda N. Ahoury, Judicael Kabas, Raïssa M. |
author_sort | Bile-Gui, Lynda N. |
collection | PubMed |
description | The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation. This disease falls within the scope of a McCune-Albright syndrome in less than 7 % of cases. The authors reported the case of a 25-year-old woman, living in the countryside, who suffered from a severe craniofacial fibrous dysplasia which has begun since her childhood with no medical care. Her clinical picture was that of McCune-Albright syndrome, and CT scan revealed advanced dysplasia with endocranial compression. |
format | Online Article Text |
id | pubmed-7569405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-75694052020-10-23 Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report Bile-Gui, Lynda N. Ahoury, Judicael Kabas, Raïssa M. Eur J Radiol Open Article The fibrous dysplasia of bone is painless, benign, and slowly progressive bone lesion. It may rarely become aggressive by compression of adjacent organs or malignant transformation. This disease falls within the scope of a McCune-Albright syndrome in less than 7 % of cases. The authors reported the case of a 25-year-old woman, living in the countryside, who suffered from a severe craniofacial fibrous dysplasia which has begun since her childhood with no medical care. Her clinical picture was that of McCune-Albright syndrome, and CT scan revealed advanced dysplasia with endocranial compression. Elsevier 2020-01-28 /pmc/articles/PMC7569405/ /pubmed/33102631 http://dx.doi.org/10.1016/j.ejro.2019.12.002 Text en © 2019 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Bile-Gui, Lynda N. Ahoury, Judicael Kabas, Raïssa M. Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report |
title | Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report |
title_full | Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report |
title_fullStr | Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report |
title_full_unstemmed | Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report |
title_short | Imaging of advanced craniofacial fibrous dysplasia associated with McCune-Albright syndrome: A case report |
title_sort | imaging of advanced craniofacial fibrous dysplasia associated with mccune-albright syndrome: a case report |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7569405/ https://www.ncbi.nlm.nih.gov/pubmed/33102631 http://dx.doi.org/10.1016/j.ejro.2019.12.002 |
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